A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273712



Internal ID20840752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114202764..114228714hg38UCSC Ensembl
chr7:113842819..113868769hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3825951
hg1925951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560530
Supporting Variants
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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